EP1801110A1 - Sel d'arginine d'ésoméprazole - Google Patents

Sel d'arginine d'ésoméprazole Download PDF

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Publication number
EP1801110A1
EP1801110A1 EP05028252A EP05028252A EP1801110A1 EP 1801110 A1 EP1801110 A1 EP 1801110A1 EP 05028252 A EP05028252 A EP 05028252A EP 05028252 A EP05028252 A EP 05028252A EP 1801110 A1 EP1801110 A1 EP 1801110A1
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EP
European Patent Office
Prior art keywords
esomeprazole
salt
pellets
layer
arginine
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
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EP05028252A
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German (de)
English (en)
Inventor
Berta Kotar-Jordan
Robert Pisek
Natalija Zajc
Anamarija Vajs
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KRKA dd
Original Assignee
KRKA Tovarna Zdravil dd
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Priority to EP05028252A priority Critical patent/EP1801110A1/fr
Priority to PCT/EP2006/012477 priority patent/WO2007071444A2/fr
Priority to EP06841138A priority patent/EP1963306A2/fr
Publication of EP1801110A1 publication Critical patent/EP1801110A1/fr
Withdrawn legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants

Definitions

  • the present invention relates to esomeprazole arginine salt as well as processes for its preparation and pharmaceutical compositions containing this salt.
  • Esomeprazole is the (S) (-) enantiomer of omeprazole, a sulfoxide which has an asymmetric center at the sulfur atom and exists in form of different enantiomers.
  • the chemical name of omeprazole is 5-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)-methyl]sulphinyl]-1H-benzimidazole.
  • Omeprazole is in-vivo transformed into an effective inhibitor of gastric acid secretion and is therefore useful as an anti-ulcer agent or for preventing and/or treating gastric acid related disorders and gastrointestinal inflammatory diseases in mammals.
  • omeprazole may be used to prevent and/or treat gastritis, gastric ulcer and duodenal ulcer.
  • Omeprazole, and its therapeutically acceptable alkaline salts are disclosed in EP 5 129 and EP 124 95 , respectively.
  • DE 4035455 discloses the separation of the enantiomers of omeprazole using a diastereomeric ether.
  • WO 94/27988 discloses certain salts, namely Na+, Mg2+, Li+, K+, Ca2+ and N(R) 4 + salts, wherein R is an alkyl with 1-4 carbon atoms, of the single enantiomers of omeprazole and their preparation. These compounds are said to have improved pharmacokinetic properties which give an improved therapeutic profile, such as a lower degree of variation between individuals taking the compound.
  • WO 98/54171 describes magnesium esomeprazole trihydrate
  • WO 00/44744 describes specific polymorphs of the potassium salt of esomeprazole
  • WO 2003/74514 discloses some primary amine salts of esomeprazole
  • WO 2004/037253 describes certain alkali metal or amine salts of esomeprazole
  • WO 2004/99182 and WO 2004/99181 disclose zinc and barium salts of esomeprazole, respectively
  • WO2005023796 discloses adamantan ammonium salts of omeprazole and esomeprazole
  • WO2005023797 describes the 1-cyclohexyl ethyl ammonium salt of inter alia esomeprazole.
  • EP 1 018 340 describes amino acid salts compounds of benzimidazole derivatives and their inclusion complexes with cyclodextrins.
  • the amorphous L-arginine omeprazole salt is described which is produced by spray drying.
  • esomeprazole arginine salt is described.
  • the present invention meets this need by providing the esomeprazole arginine salt according to claims 1 to 3.
  • the invention also relates to the process for preparing this salt according to claims 4 to 7 and pharmaceutical compositions comprising this salt according to claims 8 to 13.
  • the invention provides the esomeprazole arginine salt. It is a salt of the know drug esomeprazole with the amino acid arginine and could also be referred to as arginine esomeprazole salt. Surprisingly, this salt shows a very high stability and is therefore very suitable to be included in pharmaceutical compositions.
  • the molar ratio between esomeprazole and arginine is about 1:1 and that arginine is L-arginine.
  • the salt is in amorphous form as this may facilitate its processing into pharmaceutical compositions.
  • the salt has been characterized by its FT-IR spectrum, X-ray powder diffraction pattern and 1 H-NMR spectrum and analysed in accordance with the article »Enantioselective Analysis of Omeprazole in Pharmaceutical Formulations by Chiral High-Performance Liquid Chromatography and Capillary Electrophoresis « ( J. Braz. Chem. Soc., Vol. 15, No. 2, 318-323, 2004 ).
  • FT-IR spectra of KBr discs including the salt according to the invention were recorded over a wave number range of 4000 - 400 cm -1 on a Perkin Elmer Spectrum GX FT-IR spectrometer at a resolution of 4 cm -1 .
  • X-ray powder diffraction patterns were obtained by using a Phillips PW3040/60 X'Pert PRO powder diffractometer; CuK ⁇ radiation 1.541874 ⁇ , 3 ⁇ 2 ⁇ 31°.
  • the 1 H-NMR spectrum has been recorded by means of a Varian UNITY+ 300 spectrometer at 300 MHz using DMSO-d6 and tetramethyl silane as internal standard.
  • Figure 1 shows the X-ray powder diffractogram and Figure 2 the FT-IR spectrum of amorphous esomeprazole arginine salt.
  • the salt according to the invention is preferably prepared by a process, wherein esomeprazole and arginine are reacted in a solvent and the solvent is removed.
  • the solvent is in particular selected from water, an alcohol or a mixture thereof.
  • the preferred alcohol is methanol, ethanol, 2-propanol, n-propanol or butanol.
  • the process is carried out until all esomeprazole was dissolved or the pH value of the reaction mixture remained constant.
  • the molar ratio between the esomprazole and the arginine can vary, but is preferably about 1:1.
  • esomeprazole is dissolved in the selected solvent and then arginine is added. After completion of the reaction the solvent is removed by for example distillation, distillation under vacuum, evaporation, spray drying, and freeze drying.
  • the esomeprazole used in the process according to the invention can be prepared according to any desired method, many of which are known to those of ordinary skill in the art. Examples of suitable methods to manufacture esomeprazole are given by EP 5 129 , EP 124 495 , EP 533 752 , DE 40 35 455 , EP 652 872 , EP 707 580 , EP 773 940 , EP 795 024 , EP 836 601 , EP 897 386 , EP 946 547 , EP 984 957 , EP 964 859 , EP 1 004 305 , EP 1 095 037 , EP 1 104 417 , EP 1 230 237 , EP 1 409 478 , EP 1 458 709 , WO 03/08940 , EP 1 375 497 , WO 2004/2982 , WO 2004/52882 , WO 2004/87702 , EP 1 375 497 , WO 2005/54228 , and WO 2005/11
  • the invention also relates to pharmaceutical compositions which comprise the salt according to the invention. These compositions may be used for the treatment of gastric-acid related diseases by inhibition of gastric acid secretion.
  • compositions according to the invention are preferably in the form of pellets or tablets, in particular those which have an enteric coating layer.
  • the pellets can be filled into hard gelatine capsules or sachets which hence also represent preferred embodiments of the composition.
  • the tables can be prepared from the pellets or from a powder mixture.
  • the pellets preferably comprise
  • the tablets preferably comprise
  • the salt is included in the core in form of a layer covering the core.
  • the invention also relates to multiple-unit tablets which are obtainable by compressing a mixture of the pellets with tablet excipients.
  • Preferred pellets comprises a pellet core, optionally a separating coating, an enteric coating and optionally an over-coating as follows.
  • the core is prepared from powders comprising esomeprazole arginine and at least one pharmaceutically acceptable excipient by extrusion-spheronization or direct pelletization in a high-shear mixer or a rotor granulator.
  • the core can also be formed by applying a layer containing esomeprazole arginine to an inert bead.
  • the most preferred bead is one prepared from starch and sucrose, even though beads of other pharmaceutically acceptable excipients may be used, such as microcrystalline cellulose, vegetable gums, waxes and the like.
  • the size of the beads may vary between approximately 0.1 and 2 mm.
  • a convenient manner of coating the beads with esomeprazole arginine salt is the "powder layering" process in centrifugal equipment, i.e. rotor fluid bed equipment (Glatt Rotor Granulator), or a coating pan, i.e. a conventional coating pan (Pellegrini Coating Pan, GS Coating System).
  • the inert beads are moistened with a solution of binder, and then the active substance together with other excipients is added as a powder and the layered pellets are dried in the same equipment in which the coating is performed or other specialized equipment for drying, such as a drying chamber with or without vacuum, is used.
  • the layer with esomeprazole arginine salt can also be formed in the "suspension layering" or “solution layering” process by spraying the esomeprazole arginine suspension or solution onto the inert cores in a fluid bed coater granulator.
  • Organic solvents or water can be used during this process.
  • the core and in particular the layer with the active ingredient, comprises, besides esomeprazole arginine salt, at least one excipient selected from stabilizers, fillers, disintegrating agents, wetting agents, binders or other pharmaceutically acceptable ingredients, alone or in mixtures.
  • the stabilizer is preferably chosen among substances, such as sodium, potassium, calcium, magnesium and aluminium salts of phosphoric acid, carbonic acid, citric acid or other suitable weak inorganic or organic acids, aluminium hydroxide/sodium bicarbonate coprecipitate, aluminium, calcium and magnesium hydroxides, magnesium oxide or composite substances, such as Al 2 O 3 ⁇ 6MgO ⁇ CO 2 ⁇ 12H 2 O, (Mg 6 Al 2 (OH) 16 CO 3 ⁇ 4H 2 O), MgO ⁇ Al 2 O 3 ⁇ 2SiO 2 ⁇ nH 2 O or similar compounds, sodium lauryl sulphate, alkaline reacting amino acids and their salts or other similar, pharmaceutically acceptable pH-buffering substances.
  • substances such as sodium, potassium, calcium, magnesium and aluminium salts of phosphoric acid, carbonic acid, citric acid or other suitable weak inorganic or organic acids, aluminium hydroxide/sodium bicarbonate coprecipitate, aluminium, calcium and magnesium hydroxides, magnesium oxide or composite
  • the filler is preferably selected from the group consisting of microcrystalline cellulose, sucrose, starch, lactose, mannitol, sorbitol and mixtures thereof.
  • the disintegrating agent is preferably selected from the group consisting of starch, starch derivatives such as sodium starch glycolate or pregelatinized starch, low-substituted hydroxypropyl cellulose, crospovidone, croscarmelose sodium and mixtures thereof.
  • the wetting agent is preferably selected from the group consisting of sodium dodecyl sulphate, polyoxyethylene sorbitan fatty acid esters, poloxamers and mixtures thereof.
  • the binder is preferably selected from the group consisting of polyvinylpyrrolidone, hydroxypropyl cellulose, hydroxypropyl methylcellulose, hydroxyethyl cellulose, methylcellulose and mixtures thereof.
  • said pellets Before applying the enteric coating layer onto the cores present in form of individual pellets, said pellets may optionally be covered with one or more separating layers comprising pharmaceutical excipients optionally including alkaline compounds, such as for instance pH-buffering compounds.
  • This layer/these layers separate(s) the core material from the outer enteric coating layer.
  • the separating layer can be applied to the core by a coating or layering process in a suitable equipment such as a coating pan, coating granulator or in a fluid bed apparatus using water and/or organic solvents for the coating process.
  • the separating layer can be applied to the core by using the powder coating technique.
  • the materials for separating layers are pharmaceutically acceptable compounds, such as sugar, polyethylene glycol, polyvinylpyrrolidone, polyvinyl alcohol, polyvinyl acetate, hydroxypropyl cellulose, methylcellulose, ethylcellulose, hydroxypropyl methylcellulose, carboxymethylcellulose sodium and others, used alone or in mixtures.
  • Additives such as plasticizers, colorants, pigments, fillers, anti-tacking agents and anti-static agents, such as for instance magnesium stearate, titanium dioxide, talc and other additives may also be included in the separating layer.
  • the separating layer may serve as a diffusion barrier and may act as a pH-buffering zone.
  • the pH-buffering properties of the separating layer can be further strengthened by introducing into the layer substances chosen from a group of compounds usually used in antacid formulations, such as magnesium oxide, hydroxide or carbonate, aluminium or calcium hydroxide, carbonate or silicate, composite aluminium/magnesium compounds, such as Al 2 O 3 ⁇ 6MgO ⁇ CO 2 ⁇ 12H 2 O, (Mg 6 Al 2 (OH) 16 CO 3 ⁇ 4H 2 O), MgO ⁇ Al 2 O 3 ⁇ 2SiO 2 ⁇ nH 2 O, aluminium hydroxide/sodium bicarbonate coprecipitates or similar compounds, or other pharmaceutically acceptable pH-buffering compounds, such as the sodium, potassium, calcium, magnesium and aluminium salts of phosphoric, carbonic, citric or other suitable, week, inorganic or organic acids, or suitable organic bases, including basic amino acids and salts thereof.
  • the optionally applied separating layer is not essential for the compositions according to the invention.
  • the separating layer may improve the chemical stability of the active substance and/or the physical properties of the final dosage form.
  • the separating layer may also protect the enteric coating layer towards cracking during a compaction process.
  • the separating layer preferably contains pharmaceutically acceptable plasticizers to obtain the desired mechanical properties, such as flexibility and hardness.
  • plasticizers are for example triacetin, citric acid esters, phthalic acid esters, dibutyl sebacate, dimethyl polysiloxan, cetyl alcohol, stearyl alcohol, polyethylene glycols, propylenglycole, polysorbates or other plasticizers.
  • the mechanical properties, i.e. flexibility and hardness of the separating layer are adjusted so that the acid resistance of the pellets covered with enteric coating layer does not decrease significantly during the compression of pellets into tablets.
  • the amount of plasticizer is usually 10-50 % by weight of the separating layer forming material.
  • Additives such as dispersants, colorants, pigments, polymers, anti-tacking agent and antifoaming agents may also be included into the separating layer.
  • the maximum thickness of the applied separating layer is normally only limited by processing conditions.
  • enteric coated layers are applied onto the core or onto the core covered with separating layer(s) by using a suitable coating technique.
  • the enteric coating layer material may be dispersed or dissolved in either water or in suitable organic solvents and is preferably comprising a polymer.
  • enteric coating layer polymers one or more, separately or in combination, of the following can be used: solutions or dispersions of methacrylic acid copolymers, cellulose acetate phthalate, hydroxypropyl methylcellulose phthalate, hydroxypropyl methylcellulose acetate succinate, polyvinyl acetate phthalate, cellulose acetate trimellitate, carboxymethylethylcellulose, shellac or other suitable enteric coating layer polymer(s).
  • the enteric coating layers can also contain pharmaceutically acceptable plasticizers to obtain the desired mechanical properties, such as flexibility and hardness.
  • plasticizers are for example those mentioned above under 2.
  • the amount of plasticizer is optimized for each enteric coating layer formula, in relation to the selected enteric coating layer polymer(s), selected plasticizer(s) and the applied amount of said polymer(s), in such a way that the mechanical properties, i.e. flexibility and hardness of the enteric coating layer(s) are adjusted so that the acid resistance of the pellets covered with enteric coating layer(s) does not decrease significantly during a compression of the pellets into tablets.
  • the amount of plasticizer is usually 10-50 % by weight of the enteric coating layer polymer(s).
  • Additives such as dispersants, colorants, pigments, polymers, anti-tacking agent and antifoaming agents may also be included into the enteric coating layer(s). Other compounds may be added to increase film thickness and to decrease diffusion of acidic gastric juices into the acid susceptible material.
  • the enteric coating layer(s) usually have a thickness of about at least 10 ⁇ m, preferably more than 20 ⁇ m.
  • the maximum thickness of the applied enteric coating layer(s) is normally only limited by processing conditions.
  • the enteric coated pellets can optionally be covered with one or more over-coating layers.
  • the over-coating layer can be applied to the enteric coating layered pellets by coating or layering procedures in a suitable equipment, such as a coating pan, a coating granulator or in a fluidized bed apparatus using water and/or organic solvents for the coating process.
  • the materials for the over-coating layer are chosen among pharmaceutically acceptable compounds, such as sugar, polyethylene glycol, polyvinylpyrrolidone, polyvinyl alcohol, polyvinyl acetate, hydroxypropyl cellulose, methylcellulose, ethylcellulose, hydroxypropyl methylcellulose, microcrystalline cellulose, carboxymethylcellulose sodium and others, used alone or in mixtures.
  • Additives such as plasticizers, colorants, pigments, fillers, anti-tacking agents and anti-static agents, such as magnesium stearate, titanium dioxide, talc and other additives may also be included into the over-coating layer.
  • the over-coating layer may further prevent potential agglomeration of enteric coating layered pellets and further enhance a subsequent tableting process.
  • the over-coating layer may also protect the enteric coating layer towards cracking during a compaction process.
  • the over-coating layer contains pharmaceutically acceptable plasticizers to obtain the desired mechanical properties, such as flexibility and hardness.
  • plasticizers are for example triacetin, citric acid esters, phthalic acid esters, dibutyl sebacate, dimethyl polysiloxan, cetyl alcohol, stearyl alcohol, polyethylene glycols, propylenglycole, polysorbates or other plasticizers.
  • the amount of plasticizer is usually 10-50 % by weight of the over-coating layer forming material.
  • Additives such as dispersants, colorants, pigments, polymers, anti-tacking agent and antifoaming agents may also be included into the over-coating layer.
  • the maximum thickness of the applied over-coating layer is normally only limited by processing conditions.
  • the pellets according to the invention can be used for the preparation of multiple unit tablets.
  • enteric coated pellets with or without an over-coating layer are mixed with tablet excipients, such as fillers, binders, disintegrating agents, lubricants and other pharmaceutically acceptable additives, and compressed into tablets.
  • tablet excipients such as fillers, binders, disintegrating agents, lubricants and other pharmaceutically acceptable additives
  • the compressed tablet is optionally covered with a film forming agent to obtain a smooth surface of the tablet and further enhance the stability of the tablet during packaging and transport.
  • the pharmaceutical composition is in form of tablets which comprise a tablet core, optionally a separating coating , and an enteric coating.
  • the tablet cores are prepared from powder mixtures comprising the active substance and at least one pharmaceutically acceptable excipient by using the process of direct compression. Alternatively, said tablet cores can also be formed in the process of wet- or dry-granulation.
  • the tablet cores comprise, besides esomeprazole arginine salt, at least one excipient selected from stabilizers, fillers, disintegrating agents, wetting agents, binders or other pharmaceutically acceptable ingredients, alone or in mixtures.
  • the stabilizer is preferably chosen among substances such as sodium, potassium, calcium, magnesium and aluminium salts of phosphoric acid, carbonic acid, citric acid or other suitable weak inorganic or organic acids, aluminium hydroxide/sodium bicarbonate coprecipitates, aluminium, calcium and magnesium hydroxides, magnesium oxide or composite substances such as Al 2 O 3 ⁇ 6MgO ⁇ CO 2 ⁇ 12H 2 O, (Mg 6 Al 2 (OH) 16 CO 3 ⁇ 4H 2 O), MgO ⁇ Al 2 O 3 ⁇ 2SiO 2 ⁇ nH 2 O or similar compounds, sodium lauryl sulphate, alkaline reacting amino acids and their salts or other similar, pharmaceutically acceptable pH-buffering substances.
  • substances such as sodium, potassium, calcium, magnesium and aluminium salts of phosphoric acid, carbonic acid, citric acid or other suitable weak inorganic or organic acids, aluminium hydroxide/sodium bicarbonate coprecipitates, aluminium, calcium and magnesium hydroxides, magnesium oxide or composite
  • the filler is preferably selected from the group consisting of microcrystalline cellulose, sucrose, starch, lactose, mannitol, sorbitol and mixtures thereof.
  • the disintegrating agent is preferably selected from the group consisting of starch, starch derivatives such as sodium starch glycolate or pregelatinized starch, low-substituted hydroxypropyl cellulose, crospovidone, croscarmelose sodium and mixtures thereof.
  • the wetting agent is preferably selected from the group consisting of sodium dodecyl sulphate, polyoxyethylene sorbitan fatty acid esters, poloxamers and mixtures thereof.
  • the binder is preferably selected from the group consisting of polyvinylpyrrolidone, hydroxypropyl cellulose, hydroxypropyl methylcellulose, hydroxyethyl cellulose, methylcellulose and mixtures thereof.
  • said tablet cores may optionally be covered with one or more separating layers comprising pharmaceutical excipients optionally including alkaline compounds, such as pH-buffering compounds.
  • This layer/these layers separate(s) the core material from the outer enteric coating layer.
  • the separating layer can be applied to the core by a coating or layering process in a suitable equipment, such as a coating pan, a coating granulator or in a fluid bed apparatus using water and/or organic solvents for the coating process.
  • the separating layer can be applied to the tablet core by using a suitable coating technique.
  • the materials for separating layers are pharmaceutically acceptable compounds, such as sugar, polyethylene glycol, polyvinylpyrrolidone, polyvinyl alcohol, polyvinyl acetate, hydroxypropyl cellulose, methylcellulose, ethylcellulose, hydroxypropyl methylcellulose, carboxymethylcellulose sodium and others, used alone or in mixtures.
  • Additives such as plasticizers, colorants, pigments, fillers, anti-tacking agents and anti-static agents, such as magnesium stearate, titanium dioxide, talc and other additives may also be included into the separating layer.
  • the separating layer may serve as a diffusion barrier and may act as a pH-buffering zone.
  • the pH-buffering properties of the separating layer can be further strengthened by introducing into the layer substances chosen from a group of compounds usually used in antacid formulations, such as magnesium oxide, hydroxide or carbonate, aluminium or calcium hydroxide, carbonate or silicate, composite aluminium/magnesium compounds, such as Al 2 O 3 ⁇ 6MgO ⁇ CO 2 ⁇ 12H 2 O, (Mg 6 Al 2 (OH) 16 CO 3 ⁇ 4H 2 O), MgO ⁇ Al 2 O 3 ⁇ 2SiO 2 ⁇ nH 2 O, aluminium hydroxide/sodium bicarbonate coprecipitates or similar compounds, or other pharmaceutically acceptable pH-buffering compounds, such a the sodium, potassium, calcium, magnesium and aluminium salts of phosphoric, carbonic, citric or other suitable, week, inorganic or organic adds, or suitable organic bases, including basic amino acids and salts thereof.
  • the optionally applied separating layer is not essential for the tablets according to the invention. However, the separating layer may improve the chemical stability of the active substance and/or the physical properties of the tablet.
  • enteric coating layers are applied onto the tablet cores or onto the tablet cores covered with separating layer(s) by using a suitable coating technique.
  • the enteric coating layer material may be dispersed or dissolved in either water or in suitable organic solvents and is preferably comprising a polymer.
  • enteric coating layer polymers one or more, separately or in combination, of the following can be used: solutions or dispersions of methacrylic acid copolymers, cellulose acetate phthalate, hydroxypropyl methylcellulose phthalate, hydroxypropyl methylcellulose acetate succinate, polyvinyl acetate phthalate, cellulose acetate trimellitate, carboxymethylethylcellulose, shellac or other suitable enteric coating layer polymer(s).
  • the enteric coating layers may contain pharmaceutically acceptable plasticizers to obtain the desired mechanical properties, such as flexibility and hardness of the enteric coating layers.
  • plasticizers are for the instance, but not restricted to, triacetin, citric acid esters, phthalic acid esters, dibutyl sebacate, dimethyl polysiloxan, cetyl alcohol, stearyl alcohol, polyethylene glycols, propylenglycole, polysorbates or other plasticizers.
  • the amount of plasticizer is optimized for each enteric coating layer formula, in relation to selected enteric coating layer polymer(s), selected plasticizer(s) and the applied amount of said polymer(s), in such a way that the mechanical properties, i.e. flexibility and hardness of the enteric coating layer(s) are adjusted.
  • the amount of plasticizer is usually 10-50 % by weight of the enteric coating layer polymer(s).
  • Additives such as dispersants, colorants, pigments, polymers, anti-tacking agent and antifoaming agents may also be included into the enteric coating layer(s).
  • Other compounds may be added to increase film thickness and to decrease diffusion of acidic gastric juices into the acid susceptible material.
  • the enteric coating layer(s) constitutes a thickness of about at least 10 ⁇ m, preferably more than 20 ⁇ m.
  • the maximum thickness of the applied enteric coating layer(s) is normally only limited by processing conditions.
  • the amorphous form of the salt was indicated by the X-ray powder diffraction pattern and DSC (plain halo effect and glass transition at about 40°C).
  • the esomeprazole arginine salt was obtained from the above solution by spray drying.
  • a drug suspension was prepared using esomeprazole arginine salt, hydroxypropyl methylcellulose, magnesium carbonate, sodium lauryl sulphate and purified water. Suspension layering of sugar spheres was performed in a fluid bed processor using bottom spray technique (Wurster column). The spray operation was stopped when the specified amount of bulk liquid had been sprayed.
  • the prepared core material was dried until the loss on drying of the pellets was about 1-1.5 % and covered with a separating layer in a Wurster column with a hydroxypropyl methylcellulose solution containing talc, dibasic sodium phosphate and magnesium stearate.
  • the enteric coating suspension was prepared using methacrylic acid ethyl acrylate copolymer (Eudragit L 30 D-55), triethyl citrate, glyceryl monostearate and Polysorbate 80.
  • the suspension was sprayed onto the pellets covered with separating layer in a fluid bed apparatus. The spray operation was stopped when the specified amount of bulk liquid had been sprayed, and then drying was carried in the Wurster column.
  • the resulting pellets were classified by sieving. Microcrystalline cellulose and sodium stearyl fumarate were added and the mixture was compressed into tablets using a rotary tableting machine.
  • Enteric coated pellets / EXTRUSION & SPHERONIZATION Ingredients Composition Core material Esomeprazole arginine salt 28 % Mannitol 44.7 % Hydroxypropyl cellulose 4.5 % Microcrystalline cellulose 12.2 % Magnesium carbonate 10.2 % Sodium lauryl sulphate 0.4 % Separating layer Core material 88.9 % Hydroxypropyl methylcellulose 8.7 % Magnesium carbonate 2.4 % Enteric coating Pellets with separating layer 60.3 % Methacrylic acid ethyl acrylate copolymer 31 % Ethyl acrylate methyl methacrylate copolymer 3 % Propylenglycole 4 % Glyceryl monostearate 1.5 % Polysorbate 80 0.2 % Overcoating Pellets with enteric coating 92 % Hydroxypropyl methylcellulose 3.5 % Microcrystalline cellulose 3.5 % Polyethylene glycol 6000 1 % Tablets Pellets with overcoating 40
  • Esomeprazole arginine, mannitol, hydroxypropyl cellulose, microcrystalline cellulose and magnesium carbonate were premixed in a mixer. By adding an aqueous solution of sodium lauryl sulphate the mass was wet-mixed to a proper consistency. The wet mass was pressed through an extruder and spheronized to pellets. The pellets were dried in a fluid bed dryer until the loss on drying was about 1-1.5 %, and then they were classified by sieving.
  • the prepared core material was covered with a separating layer.
  • Magnesium carbonate was suspended in a hydroxypropyl methylcellulose solution and the dispersion was sprayed onto agitated pellets in a Wurster column.
  • the enteric coating layer was applied to the pellets covered with separating layer using an aqueous dispersion of methacrylic acid ethyl acrylate copolymer (Eudragit L 30 D-55) and ethyl acrylate methyl methacrylate copolymer (Eudragit NE 30 D) plasticized with propylenglycole to which a glyceryl monostearate dispersion had been added.
  • the suspension was sprayed onto the pellets covered with the separating layer in a Wurster column until the specified amount of bulk liquid had been sprayed. The drying process was carried out in the same equipment.
  • Additional coating was applied in a Wurster column by spraying a dispersion of hydroxypropyl methylcellulose, microcrystalline cellulose and polyethylene glycol on the enteric-coated pellets.
  • the resulting pellets were dried, classified by sieving and compressed into tablets together with microcrystalline cellulose and sodium stearyl fumarate using a rotary tableting machine.
  • Enteric coated tablets Ingredients Composition Tablet core Esomeprazole arginine salt 10.8 % Lactose 61.6 % Hydroxypropyl cellulose 2.8 % Hydroxypropyl cellulose (low substitution) 3.9 % Talc 2.7 % L-arginine 3.6 % Magnesium stearate 1 % Separating layer Hydroxypropyl methylcellulose 1.9 % Talc 0.9 % Magnesium hydroxide 0.7 % Enteric coating layer Hydroxypropyl methylcellulose phthalate 7.1 % Talc 1.1 % Titanium dioxide 1 % Diethyl phthalate 0.9 %
  • the following powders were mixed together: lactose, esomeprazole arginine salt, hydroxypropyl cellulose (low degree of substitution), talc and L-arginine. Hydroxypropyl cellulose was dissolved in a sufficient quantity of purified water and used as granulation liquid for the powder mixture. After the granulation, the granules were dried, sieved, magnesium stearate was added and tablets were prepared by compressing the granules using a rotary compression machine.
  • the tablet cores were further coated with a separating layer.
  • the isopropyl alcohol/methylene chloride dispersion of hydroxypropyl methylcellulose, magnesium hydroxide and talc was sprayed onto the tablets in a suitable coating pan until a desired weight gain was reached. The drying was carried out in the coating pan.
  • Such coated tablets were loaded in a perforated coating pan to be further coated with an enteric layer.
  • An enteric coating suspension was prepared by dispersing hydroxypropyl methylcellulose phthalate, talc, titanium dioxide and diethyl phthalate in the mixture of methanol and methylene chloride. The enteric coating suspension was sprayed simultaneously. The spraying operation was stopped when the specified amount of liquid had been sprayed, and then drying was carried out in the coating pan.

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EP05028252A 2005-12-22 2005-12-22 Sel d'arginine d'ésoméprazole Withdrawn EP1801110A1 (fr)

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EP05028252A EP1801110A1 (fr) 2005-12-22 2005-12-22 Sel d'arginine d'ésoméprazole
PCT/EP2006/012477 WO2007071444A2 (fr) 2005-12-22 2006-12-22 Esomeprazole arginine
EP06841138A EP1963306A2 (fr) 2005-12-22 2006-12-22 Esomeprazole arginine

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EP05028252A EP1801110A1 (fr) 2005-12-22 2005-12-22 Sel d'arginine d'ésoméprazole

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010097583A1 (fr) 2009-02-24 2010-09-02 Cipla Limited Polymorphe de l'ésoméprazole de potassium et sa préparation
WO2010148314A2 (fr) * 2009-06-19 2010-12-23 Dr. Reddy's Laboratories Ltd. Préparation d'ésoméprazole et de ses sels pharmaceutiquement acceptables
EP2331084A1 (fr) * 2008-10-06 2011-06-15 Jubilant Life Sciences Limited Compositions pharmaceutiques comprenant de l ésoméprazole amorphe, formes pharmaceutiques et procédé associés

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102008045339A1 (de) * 2008-09-01 2010-03-04 Stada Arzneimittel Ag Pharmazeutisches Pellet
EP2499125B1 (fr) 2009-11-12 2016-01-27 Hetero Research Foundation Procédé de dédoublement de l'oméprazole

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EP0012495A1 (fr) 1978-12-08 1980-06-25 Beecham Group Plc Composition pharmaceutique comprenant un sel hydrosoluble d'amoxycilline et polyvinylpyrrolidone, et une ampoule contenant une dose unitaire de cette composition
EP0124495A2 (fr) 1983-03-04 1984-11-07 Aktiebolaget Hässle Sels d'oméprazole
DE4035455A1 (de) 1990-11-08 1992-05-14 Byk Gulden Lomberg Chem Fab Enantiomerentrennung
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EP1230237A1 (fr) 1999-11-16 2002-08-14 SHERMAN, Bernard Charles Omeprazole magnesien
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WO2003074514A1 (fr) 2002-03-05 2003-09-12 Astrazeneca Ab Sels d'alkylammonium d'omeprazole et d'esomeprazole
EP1375497A1 (fr) 2002-05-17 2004-01-02 Bernard Charles Sherman Sel de magnésium de S-omeprazole
WO2004002982A2 (fr) 2002-06-27 2004-01-08 Dr. Reddy's Laboratories Limited Procede de preparation de composes sulfoxyde optiquement purs ou optiquement enrichis, notamment de l'esomeprazole amorphe et ses sels
EP1409478A1 (fr) 2001-07-16 2004-04-21 Janssen Pharmaceutica N.V. Procede ameliore de preparation de composes de type benzimidazole
WO2004037253A1 (fr) 2002-10-22 2004-05-06 Ranbaxy Laboratories Limited Forme amorphe de sels d'esomeprazole
WO2004052882A1 (fr) 2002-12-06 2004-06-24 Altana Pharma Ag Procede de preparation de composes actifs optiquement pures
EP1458709A1 (fr) 2001-12-18 2004-09-22 AstraZeneca AB Procede de preparation d'enantiomeres enrichis au niveau optique au moyen d'une chromatographie a lit mobile simule
WO2004087702A2 (fr) 2003-03-28 2004-10-14 Sidem Pharma Procede de preparation enantioselective de derives de sulfoxydes.
WO2004099181A1 (fr) 2003-05-05 2004-11-18 Ranbaxy Laboratories Limited Sel de baryum d'un derive de benzimidazole
WO2004099182A1 (fr) 2003-05-05 2004-11-18 Ranbaxy Laboratories Limited Sel de zinc de (s)-omeprazole
WO2005023797A1 (fr) 2003-09-04 2005-03-17 Astrazeneca Ab Nouveaux sels d'omeprazole et d'esomeprazole ii
WO2005023796A1 (fr) 2003-09-04 2005-03-17 Astrazeneca Ab Nouveaux sels d'omeprazole et d'esomeprazole i
WO2005054228A1 (fr) 2003-12-05 2005-06-16 Hetero Drugs Limited Procede de preparation d'enantiomeres de pyridinylmethylsulfinyl- benzamide substitues
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0005129A1 (fr) 1978-04-14 1979-10-31 Aktiebolaget Hässle Pyridylsulfinylbenzimidazoles substitués, compositions pharmaceutiques les renfermant et les intermédiaires pour leur préparation
EP0012495A1 (fr) 1978-12-08 1980-06-25 Beecham Group Plc Composition pharmaceutique comprenant un sel hydrosoluble d'amoxycilline et polyvinylpyrrolidone, et une ampoule contenant une dose unitaire de cette composition
EP0124495A2 (fr) 1983-03-04 1984-11-07 Aktiebolaget Hässle Sels d'oméprazole
EP0533752A1 (fr) 1990-06-07 1993-03-31 Astra Aktiebolag Procede de synthese ameliore
DE4035455A1 (de) 1990-11-08 1992-05-14 Byk Gulden Lomberg Chem Fab Enantiomerentrennung
WO1994027988A1 (fr) 1993-05-28 1994-12-08 Astra Aktiebolag Sels optiquement purs de composes de pyridinylmethyle sylfinyl-ih-benzimidazole
EP0652872A1 (fr) 1993-05-28 1995-05-17 Astra Aktiebolag Sels optiquement purs de composes de pyridinylmethyle sulfinyl-1h-benzimidazole
EP0707580A1 (fr) 1993-07-09 1996-04-24 Astra Aktiebolag Omeprazole de magnesium
EP0773940A1 (fr) 1994-07-15 1997-05-21 Astra Aktiebolag Procede de synthese de sulfoxydes substitues
EP0795024A1 (fr) 1994-11-28 1997-09-17 Astra Aktiebolag Preparation enantioselective de sulfoxydes actifs sur le plan pharmaceutique obtenue par bio-oxydation
EP0836601A1 (fr) 1995-07-03 1998-04-22 Astra Aktiebolag Procede de purification optique pour derives de benzimidazole enrichis par enantiomorphe
EP0897386A1 (fr) 1996-04-26 1999-02-24 Astra Aktiebolag Procede de preparation d'un sel de magnesium d'un heterocycle sulfinyl substitue
EP0946547A1 (fr) 1996-12-20 1999-10-06 Astra Aktiebolag Nouvelle forme de compose
WO1998054171A1 (fr) 1997-05-30 1998-12-03 Astra Aktiebolag Nouvelle forme de s-omeprazole
EP0984957A1 (fr) 1997-05-30 2000-03-15 Astra Aktiebolag NOUVELLE FORME DE $i(S)-OMEPRAZOLE
EP0964859A1 (fr) 1997-11-14 1999-12-22 Astra Aktiebolag Nouveau procede
EP1004305A1 (fr) 1998-04-20 2000-05-31 Eisai Co., Ltd. Compositions stabilisees contenant des composes du type benzimidazole
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EP1104417A1 (fr) 1998-08-11 2001-06-06 Merck & Co., Inc. Procede ameliore de preparation, d'isolation et de purification de l'omeprazole et compositions d'omeprazole
EP1018340A1 (fr) 1999-01-06 2000-07-12 Tecnimede-Sociedade Tecnico-Medicinal, S.A. Complexes d'inclusion de sels d'aminoacides de dérivés du benzimidazol et de cyclodextrines, leur préparation et formulations pharmaceutiques les contenant
WO2000044744A1 (fr) 1999-01-28 2000-08-03 Astrazeneca Ab Sel de potassium, de ($i(s))-omeprazole
EP1230237A1 (fr) 1999-11-16 2002-08-14 SHERMAN, Bernard Charles Omeprazole magnesien
WO2003008940A1 (fr) 2001-07-16 2003-01-30 August Technology Corporation Systeme confocal d'inspection tridimensionnelle et procede correspondant
EP1409478A1 (fr) 2001-07-16 2004-04-21 Janssen Pharmaceutica N.V. Procede ameliore de preparation de composes de type benzimidazole
EP1458709A1 (fr) 2001-12-18 2004-09-22 AstraZeneca AB Procede de preparation d'enantiomeres enrichis au niveau optique au moyen d'une chromatographie a lit mobile simule
WO2003074514A1 (fr) 2002-03-05 2003-09-12 Astrazeneca Ab Sels d'alkylammonium d'omeprazole et d'esomeprazole
EP1375497A1 (fr) 2002-05-17 2004-01-02 Bernard Charles Sherman Sel de magnésium de S-omeprazole
WO2004002982A2 (fr) 2002-06-27 2004-01-08 Dr. Reddy's Laboratories Limited Procede de preparation de composes sulfoxyde optiquement purs ou optiquement enrichis, notamment de l'esomeprazole amorphe et ses sels
WO2004037253A1 (fr) 2002-10-22 2004-05-06 Ranbaxy Laboratories Limited Forme amorphe de sels d'esomeprazole
WO2004052882A1 (fr) 2002-12-06 2004-06-24 Altana Pharma Ag Procede de preparation de composes actifs optiquement pures
WO2004087702A2 (fr) 2003-03-28 2004-10-14 Sidem Pharma Procede de preparation enantioselective de derives de sulfoxydes.
WO2004099181A1 (fr) 2003-05-05 2004-11-18 Ranbaxy Laboratories Limited Sel de baryum d'un derive de benzimidazole
WO2004099182A1 (fr) 2003-05-05 2004-11-18 Ranbaxy Laboratories Limited Sel de zinc de (s)-omeprazole
WO2005023797A1 (fr) 2003-09-04 2005-03-17 Astrazeneca Ab Nouveaux sels d'omeprazole et d'esomeprazole ii
WO2005023796A1 (fr) 2003-09-04 2005-03-17 Astrazeneca Ab Nouveaux sels d'omeprazole et d'esomeprazole i
WO2005054228A1 (fr) 2003-12-05 2005-06-16 Hetero Drugs Limited Procede de preparation d'enantiomeres de pyridinylmethylsulfinyl- benzamide substitues
WO2005116011A1 (fr) 2004-05-28 2005-12-08 Hetero Drugs Limited Nouveau procede de synthese stereoselective de sulfoxydes de benzimidazole

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2331084A1 (fr) * 2008-10-06 2011-06-15 Jubilant Life Sciences Limited Compositions pharmaceutiques comprenant de l ésoméprazole amorphe, formes pharmaceutiques et procédé associés
EP2331084A4 (fr) * 2008-10-06 2014-01-22 Jubilant Life Sciences Ltd Compositions pharmaceutiques comprenant de l ésoméprazole amorphe, formes pharmaceutiques et procédé associés
WO2010097583A1 (fr) 2009-02-24 2010-09-02 Cipla Limited Polymorphe de l'ésoméprazole de potassium et sa préparation
WO2010148314A2 (fr) * 2009-06-19 2010-12-23 Dr. Reddy's Laboratories Ltd. Préparation d'ésoméprazole et de ses sels pharmaceutiquement acceptables
WO2010148314A3 (fr) * 2009-06-19 2011-05-26 Dr. Reddy's Laboratories Ltd. Préparation d'ésoméprazole et de ses sels pharmaceutiquement acceptables

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